المؤلفون: Zollino, M.

المساهمون: Loviglio, M. N., Leleu, M., Männik, K., Passeggeri, M., Giannuzzi, G., Van Der Werf, I., Waszak, S. M., Zazhytska, M., Roberts-Caldeira, I., Gheldof, N., Migliavacca, E., Alfaiz, A. A., Hippolyte, L., Maillard, A. M., Zollino, Marcella, Van Dijck, A., Kooy, R. F., Sanlaville, D., Rosenfeld, J. A., Shaffer, L. G., Andrieux, J., Marshall, C., Scherer, S. W., Shen, Y., Gusella, J. F., Thorsteinsdottir, U., Thorleifsson, G., Dermitzakis, E. T., Deplancke, B., Beckmann, J. S., Rougemont, J., Jacquemont, S., Reymond, A.

مصطلحات موضوعية: Adolescent, Adult, Aged, Autism Spectrum Disorder, Autistic Disorder, Body Mass Index, Child, Preschool, Chromatin, Chromosome Deletion, Chromosome Duplication, Chromosome Mapping, Chromosomes, Human, Pair 16, DNA Copy Number Variation, Female, In Situ Hybridization, Fluorescence, Infant, Intellectual Disability, Male, Megalencephaly, Microcephaly, Middle Aged, Obesity, Phenotype, Molecular Biology, Psychiatry and Mental Health, Cellular and Molecular Neuroscience

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/27240531; info:eu-repo/semantics/altIdentifier/wos/WOS:000401702800007; volume:22; issue:6; firstpage:836; lastpage:849; numberofpages:14; issueyear:2017; journal:MOLECULAR PSYCHIATRY; http://hdl.handle.net/10807/114664Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84973140920; http://www.nature.com/mp/index.htmlTest

الإتاحة: https://doi.org/10.1038/mp.2016.84Test
http://hdl.handle.net/10807/114664Test
http://www.nature.com/mp/index.htmlTest

المؤلفون: Li Sun, Magdalena Zernicka-Goetz, Bailey A. T. Weatherbee, Yiping Zhan, Xin Tao, Richard T. Scott, Emre Seli, Tianren Wang, Gary D. Smith, Marta N. Shahbazi, Antonio Pellicer, Laura M Keller

المساهمون: Shahbazi, Marta N. [0000-0002-1599-5747], Weatherbee, Bailey A. T. [0000-0002-6825-6278], Seli, Emre [0000-0001-7464-8203], Zernicka-Goetz, Magdalena [0000-0002-7004-2471], Apollo - University of Cambridge Repository, Shahbazi, Marta N [0000-0002-1599-5747], Weatherbee, Bailey AT [0000-0002-6825-6278]

المصدر: Nature Communications, Vol 11, Iss 1, Pp 1-15 (2020)
Nature Communications

مصطلحات موضوعية: 0301 basic medicine, Embryology, 631/136/1455, Chromosomes, Human, Pair 21, General Physics and Astronomy, Aneuploidy, Trisomy, 02 engineering and technology, 631/136/2086/1986, 13, 14, 13/1, Monosomy, Pregnancy, Chromosome Segregation, 38/23, 38/22, 14/19, lcsh:Science, 631/80/641/2002, Multidisciplinary, Mosaicism, Stem Cells, article, Trisomy 16, 021001 nanoscience & nanotechnology, Cadherins, medicine.anatomical_structure, embryonic structures, Female, Ploidy, 0210 nano-technology, animal structures, Science, Embryonic Development, 13/106, 13/109, Biology, General Biochemistry, Genetics and Molecular Biology, 38, Andrology, 03 medical and health sciences, 13/100, Antigens, CD, medicine, Cell Adhesion, Humans, Cell Lineage, Embryo Implantation, Genetic Testing, Trophoblast, General Chemistry, Cell Cycle Checkpoints, Genes, erbB-1, medicine.disease, Embryo, Mammalian, 030104 developmental biology, lcsh:Q, Chromosome 21, Chromosomes, Human, Pair 16

وصف الملف: application/pdf; application/zip; text/xml; application/vnd.ms-excel

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d848a250031c4868f23216d53277fc0Test
http://link.springer.com/article/10.1038/s41467-020-17764-7Test

المؤلفون: Richard S. Smith, Kellen D. Winden, Hannah Pinson, Pooja Venugopal, Max Tegmark, Michael E. Talkowski, Mustafa Sahin, Christopher A. Walsh, Derek J. C. Tai, James F. Gusella, Maria Sundberg

المساهمون: Doctoraatsbegeleiding, Informatics and Applied Informatics, Data Analytics Laboratory

المصدر: Nature Communications, Vol 12, Iss 1, Pp 1-20 (2021)
Nature Communications

مصطلحات موضوعية: 0301 basic medicine, RHOA, DNA Copy Number Variations, Science, Induced Pluripotent Stem Cells, Gene Expression, General Physics and Astronomy, Biology, Synaptic Transmission, Article, General Biochemistry, Genetics and Molecular Biology, 03 medical and health sciences, Bursting, 0302 clinical medicine, mental disorders, medicine, Humans, Copy-number variation, Organic Chemicals, Stem cells in the nervous system, Induced pluripotent stem cell, Cells, Cultured, Multidisciplinary, Hyperactivation, Reverse Transcriptase Polymerase Chain Reaction, Dopaminergic Neurons, Dopaminergic, Cell Differentiation, General Chemistry, Cell biology, 030104 developmental biology, medicine.anatomical_structure, nervous system, biology.protein, Diseases of the nervous system, Soma, Neuron, Chromosome Deletion, Nerve Net, rhoA GTP-Binding Protein, Chromosomes, Human, Pair 16, 030217 neurology & neurosurgery, Neuroscience

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00c7c5c50f7937a061bf650901000804Test
https://doi.org/10.1038/s41467-021-23113-zTest

المؤلفون: Nuttle, Xander, GIANNUZZI, GIULIANA, Duyzend, Michael H., Schraiber, Joshua G., Narvaiza, Iñigo, Sudmant, Peter H., Penn, Osnat, CHIATANTE, GIORGIA, Malig, Maika, Huddleston, John, Benner, Chris, Camponeschi, Francesca, Ciofi Baffoni, Simone, Stessman, Holly A. F., Marchetto, Maria C. N., Denman, Laura, Harshman, Lana, Baker, Carl, Raja, Archana, Penewit, Kelsi, Janke, Nicolette, Joyce Tang, W., VENTURA, MARIO, BANCI, LUCIA, ANTONACCI, FRANCESCA, Akey, Joshua M., Amemiya, Chris T., Gage, Fred H., Reymond, Alexandre, Eichler, Evan E.

المساهمون: X. Nuttle, G. Giannuzzi, M.H. Duyzend, J.G. Schraiber, I. Narvaiza, P.H. Sudmant, O. Penn, G. Chiatante, M. Malig, J. Huddleston, C. Benner, F. Camponeschi, S. Ciofi Baffoni, H.A.F. Stessman, M.C.N. Marchetto, L. Denman, L. Harshman, C. Baker, A. Raja, K. Penewit, N. Janke, W. Joyce Tang, M. Ventura, L. Banci, F. Antonacci, J.M. Akey, C.T. Amemiya, F.H. Gage, A. Reymond, E.E. Eichler

مصطلحات موضوعية: Animal, Autistic Disorder, Chromosome Breakage, Chromosome, Human, Pair 16, DNA Copy Number Variation, Gene Duplication, Homeostasi, Iron, Pan troglodyte, Pongo, Protein, Recombination, Genetic, Species Specificity, Time Factor, Evolution, Molecular, Genetic Predisposition to Disease, Medicine (all), Multidisciplinary, Settore BIO/18 - Genetica

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/27487209; info:eu-repo/semantics/altIdentifier/wos/WOS:000381472100035; volume:536; issue:7615; firstpage:205; lastpage:209; numberofpages:5; journal:NATURE; http://hdl.handle.net/2434/863072Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84982113175

الإتاحة: https://doi.org/10.1038/nature19075Test
http://hdl.handle.net/2434/863072Test

المؤلفون: Nagrani R., Foraita R., Gianfagna F., Iacoviello L., Marild S., Michels N., Molnar D., Moreno L., Russo P., Veidebaum T., Ahrens W., Marron M.

المصدر: Scientific Reports, Vol 10, Iss 1, Pp 1-14 (2020)
SCIENTIFIC REPORTS
Scientific Reports
Scientific reports, 10:7189
Zaguán: Repositorio Digital de la Universidad de Zaragoza
Universidad de Zaragoza
Zaguán. Repositorio Digital de la Universidad de Zaragoza
instname
Scientific reports (Nature Publishing Group) 10 (2020): 7189. doi:10.1038/s41598-020-64031-2
info:cnr-pdr/source/autori:Nagrani R.; Foraita R.; Gianfagna F.; Iacoviello L.; Marild S.; Michels N.; Molnar D.; Moreno L.; Russo P.; Veidebaum T.; Ahrens W.; Marron M./titolo:Common genetic variation in obesity, lipid transfer genes and risk of Metabolic Syndrome: Results from IDEFICS%2FI.Family study and meta-analysis/doi:10.1038%2Fs41598-020-64031-2/rivista:Scientific reports (Nature Publishing Group)/anno:2020/pagina_da:7189/pagina_a:/intervallo_pagine:7189/volume:10

مصطلحات موضوعية: Adult, Male, FTO RS9939609 POLYMORPHISM, obesity, Pediatric Obesity, SUSCEPTIBILITY LOCI, Metabolic disorders, Alpha-Ketoglutarate-Dependent Dioxygenase FTO, lcsh:Medicine, Polymorphism, Single Nucleotide, Article, QUALITY-CONTROL, Medicine and Health Sciences, Humans, Family, GENOME-WIDE ASSOCIATION, Child, lcsh:Science, Genetic association study, Metabolic Syndrome, Multidisciplinary, COMPONENTS, lcsh:R, Diagnostic markers, Risk factors, Cholesterol Ester Transfer Proteins, WEIGHT-GAIN, meta-analysis, BODY-MASS INDEX, PHYSICAL-ACTIVITY, Child, Preschool, Female, lcsh:Q, genetic, FAT-MASS, Chromosomes, Human, Pair 16, VARIANT RS9939609

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::c06e0d3b2b31c5edfe3bdb4a8160e95fTest
http://link.springer.com/article/10.1038/s41598-020-64031-2Test

المؤلفون: Ziv, Elad, Dean, Eric, Hu, Donglei, Martino, Alessandro, Serie, Daniel, Curtin, Karen, Campa, Daniele, Aftab, Blake, Bracci, Paige, Buda, Gabriele, Zhao, Yi, Caswell-Jin, Jennifer, Diasio, Robert, Dumontet, Charles, Dudziński, Marek, Fejerman, Laura, Greenberg, Alexandra, Huntsman, Scott, Jamroziak, Krzysztof, Jurczyszyn, Artur, Kumar, Shaji, Atanackovic, Djordje, Glenn, Martha, Cannon-Albright, Lisa A, Jones, Brandt, Lee, Adam, Marques, Herlander, Martin, Thomas, Martinez-Lopez, Joaquin, Rajkumar, Vincent, Sainz, Juan, Vangsted, Annette Juul, Wątek, Marzena, Wolf, Jeffrey, Slager, Susan, Camp, Nicola J, Canzian, Federico, Vachon, Celine

المساهمون: Ziv,E, Hu,D, Caswell.Jin,J,H, Fejerman,L, Huntsman,S Division of General Internal Medicine, Department of Medicine, Institute for Human Genetics, Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, California USA. Dean,E Sutter Medical Center of Santa Rosa, Santa Rosa, California USA. Martino,A, Campa,D, Canzian,F Genomic Epidemiology Group, German Cancer Research Center (DKFZ), Heidelberg, Germany. Serie,D Division of Biomedical Statistics and Informatics. Department of Health Sciences Research, Mayo Clinic, Jacksonville, Florida USA. Curtin,K, Zhao,Y, Atanackovic,D, Glenn,M, Cannon-Albright,L, Jones,B, Camp,NJ Department of Internal Medicine, University of Utah School of Medicine, Salt Lake City, USA. Aftalb,B, Martin,T, Wolf,J Division of Hematology, Department of Medicine, Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, California USA. Bracci,P Department of Epidemiology and Biostatistics, Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, California , USA. Buda,G Department of Oncology, Transplants and Advanced Technologies, Section of Hematology, Pisa University Hospital, Pisa, Italy. Diasio,R, Lee,A Department of Molecular Pharmacology and Experimental Therapeutics, College of Medicine, Mayo Clinic, Rochester, Minnesota USA. Dumontet,C INSERM UMR 1052/CNRS 5286, Laboratoire de Cytologie Analytique, Faculte´ de Me´decine Rockefeller, Universite´ Claude Bernard Lyon I, Lyon, France. Dudzinski,M Department of Hematology, Rzeszow Regional Hospital, Rzeszow 35-301, Poland. Greenberg,A Center for Translational Science Activities, Mayo Clinic, Rochester, Minnesota 55905, USA. Greenberg,A, Vachon, C Division of Epidemiology, Department of Health Sciences Research, Mayo Clinic, Rochester, Minnesota, USA. Jamroziak,K Department of Hematology, Medical University of Lodz, Lodz, Poland. Jurczyszyn,A Department of Hematology, Cracow University Hospital, Cracow, Poland. Kumar,S, Rajkumar,V Division of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota, USA. Marques,H Life and Health Sciences Research Institute (ICVS), School of Health Sciences, University of Minho, Braga , Portugal. Martinez-Lopez,J Hematology Service, CRIS facility for Hematological research, Hospital Universitario 12 de Octubre, Universidad Complutense, Madrid, Spain. Sainz,J Genomic Oncology Area, GENYO, Centre for Genomics and Oncological Research: Pfizer/University of Granada/Andalusian Regional Government, Granada, Spain. Department of Hematology, Virgen de las Nieves University Hospital, Granada, Spain. Vangsted,AJ Department of Hematology, Righospitalet and Roskilde Hospital, Copenhagen University, Copenhagen, Denmark. Watek,M Department of Hematology, Holycross Cancer Center, Kielce, Poland. Slager,S Division of Biomedical Statistics and Informatics. Department of Health Sciences Research, Mayo Clinic College of Medicine, Rochester, Minnesota USA., This work was supported by the Steve and Nancy Grand Multiple Myeloma Translational Initiative and a grant from Expression Analysis and a grant from the National Cancer Institute (R21CA191896). E.Z. is supported in part by a mid-career award in patient research from the National Cancer Institute (K24169004). Collection of blood samples from Polish patients and controls from Łodz area, and DNA extraction was supported by a grant from Polish Ministry of Science and Higher Education (No. NN402178334). DNA extraction from Danish healthy controls was supported by The Research Fund at Region Sjælland, Denmark. The Utah study was supported by LLS 6067–09, CA152336 and CA134674, with data collection made possible, in part, by the Utah Population Database (UPDB) and the Utah Cancer Registry (UCR). Partial support for all data sets within the UPDB is provided by the Huntsman Cancer Institute (HCI) and the HCI Cancer Center Support grant, P30 CA42014. The UCR is supported in part by NIH contract HHSN261201000026C from the NCI SEER Program with additional support from the Utah State Department of Health and the University of Utah.

مصطلحات موضوعية: Genome-Wide Association Study, Humans, Kaplan-Meier Estimate, Multiple Myeloma, Polymorphism, Single Nucleotide, Chromosomes, Human, Pair 16

وصف الملف: application/pdf; application/vnd.oasis.opendocument.spreadsheet

العلاقة: http://www.nature.com/ncomms/2015/150722/ncomms8539/full/ncomms8539.htmlTest; Ziv E, Dean E, Hu D, Martino A, Serie D, Curtin K, et al. Genome-wide association study identifies variants at 16p13 associated with survival in multiple myeloma patients. Nat Commun. 2015; 6:7539; http://hdl.handle.net/10668/2290Test; PMC4656791

الإتاحة: https://doi.org/10.1038/ncomms8539Test
http://hdl.handle.net/10668/2290Test

المؤلفون: Steinberg, S, de Jong, S, Mattheisen, M, Costas, J, Demontis, D, Jamain, S, Pietiläinen, O P H, Lin, K, Papiol, S, Huttenlocher, J, Sigurdsson, E, Stefanovski, B, Durmishi, N, Pejovic Milovancevic, M, Lecic Tosevski, D, Silagadze, T, Naneishvili, N, Mikeladze, N, Surguladze, S, Vincent, J B, Farmer, A, Corvin, A, Mitchell, P B, Wright, A, Schofield, P R, Fullerton, J M, Montgomery, G W, Martin, N G, Rubino, I A, van Winkel, R, Kenis, G, De Hert, M, Gill, M, Réthelyi, J M, Bitter, I, Terenius, L, Jönsson, E G, Bakker, S, van Os, J, Jablensky, A, Leboyer, M, Bramon, E, Powell, J, Morris, D, Murray, R, O'Neill, F A, Kendler, K, Riley, B, Craddock, N, Owen, M J, O'Donovan, M C, Thorsteinsdottir, U, Vassos, E, Kong, A, Ehrenreich, H, Carracedo, A, Golimbet, V, Andreassen, O A, Børglum, A D, Mors, O, Mortensen, P B, Werge, T, Ophoff, R A, Giegling, I, Nöthen, M M, Rietschel, M, Cichon, S, Ruggeri, M, Tosato, S, Palotie, A, St Clair, D, Rujescu, D, Collier, D A, Stefansson, H, Breuer, R, Stefansson, K, Fraser, G, Walker, N, Melle, I, Djurovic, S, Agartz, I, Tuulio-Henriksson, A, Suvisaari, J, Lönnqvist, J, Paunio, T, Olsen, L, Hansen, T, Ingason, A, Pirinen, M, Strengman, E, Hougaard, D M, Orntoft, T, Didriksen, M, Hollegaard, M V, Nordentoft, M, Abramova, L, Kaleda, V, Arrojo, M, Sanjuán, J, Arango, C, Etain, B, Bellivier, F, Méary, A, Schürhoff, F, Szoke, A, Ribolsi, M, Magni, V, Siracusano, A, Sperling, S, Rossner, M, Christiansen, C, Kiemeney, L A, Franke, B, van den Berg, L H, Veldink, J, Curran, S, Bolton, P, Poot, M, Staal, W, Rehnstrom, K, Kilpinen, H, Freitag, C M, Meyer, J, Magnusson, P, Saemundsen, E, Martsenkovsky, I, Bikshaieva, I, Martsenkovska, I, Vashchenko, O, Raleva, M, Paketchieva, K

المساهمون: deCODE Genet, IS-101 Reykjavik, Iceland Univ Calif Los Angeles, Ctr Neurobehav Genet, Los Angeles, CA USA Harvard Univ, Brigham & Womens Hosp, Sch Med, Channing Div Network Med, Boston, MA 02115 USA Univ Bonn, Inst Genom Math, Bonn, Germany Univ Bonn, Dept Genom, Life & Brain Ctr, Bonn, Germany CHUS, Galician Fdn Genom Med SERGAS, Santiago De Compostela, Spain Aarhus Univ, Dept Biomed, Aarhus, Denmark Aarhus Univ, iSEQ, Ctr Integrat Sequencing, Aarhus, Denmark Lundbeck Fdn Initiat Integrat Psychiat Res, iPSYCH, Aarhus, Denmark Fdn FondaMental, Creteil, France Hop Henri Mondor, INSERM, U955, F-94010 Creteil, France Univ Helsinki, Inst Mol Med Finland FIMM, Helsinki, Finland Inst Hlth & Welf, Publ Hlth Genom Unit, Helsinki, Finland Wellcome Trust Sanger Inst, Cambridge, England South London & Maudsley NHS Fdn Trust, NIHR Biomed Res Ctr Mental Hlth, Dept Neurosci, London, England Kings Coll London, London, England DFG Res Ctr Mol Physiol Brain CMPB, Gottingen, Germany Max Planck Inst Expt Med, Div Clin Neurosci, D-37075 Gottingen, Germany Univ Tubingen, Inst Human Genet, Dept Med Genet, Tubingen, Germany Natl Univ Hosp Reykjavik, Dept Psychiat, Reykjavik, Iceland Univ Iceland, Sch Med, Reykjavik, Iceland Kings Coll London, Inst Psychiat, Social Genet & Dev Psychiat Res Ctr, London, England Univ Munich, Dept Psychiat, Div Mol & Clin Neurobiol, D-80539 Munich, Germany Heidelberg Univ, Cent Inst Mental Hlth, Dept Genet Epidemiol Psychiat, Mannheim, Germany Univ Aberdeen, Dept Mental Hlth, Royal Cornhill Hosp, Aberdeen, Scotland Ravenscraig Hosp, Greenock, Scotland Univ Oslo, Inst Clin Med, KG Jebsen Ctr Psychosis Res, Div Mental Hlth & Addict,Oslo Univ Hosp, Oslo, Norway Natl Inst Hlth & Welf, Dept Mental Hlth & Subst Abuse Serv, Helsinki, Finland Univ Helsinki, Dept Psychiat, SF-00180 Helsinki, Finland Univ Helsinki, Cent Hosp, Helsinki, Finland Natl Inst Hlth & Welf THL, Publ Hlth Genom Unit, Helsinki, Finland Univ Copenhagen, Mental Hlth Ctr Sct Hans, Inst Biol Psychiat, Roskilde, Denmark Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford, England Univ Med Ctr Utrecht, Dept Med Genet, Utrecht, Netherlands Statens Serum Inst, Dept Clin Biochem Immunol & Genet, Sect Neonatal Screening & Hormones, DK-2300 Copenhagen, Denmark Aarhus Univ Hosp, Dept Mol Med, DK-8000 Aarhus, Denmark H Lundbeck & Co AS, Synapt Transmiss, Copenhagen, Denmark Copenhagen Univ Hosp, Psychiat Ctr Copenhagen, Copenhagen, Denmark Russian Acad Med Sci, Mental Hlth Res Ctr, Moscow 109801, Russia CHUS, Serv Psychiat, Santiago De Compostela, Spain Univ Valencia, Network Ctr Biomed Res Mental Hlth CIBERSAM, Unit Psychiat, Fac Med, Valencia, Spain Univ Complutense, Hosp Gen Univ Gregorio Maranon, IiSGM, CIBERSAM, E-28040 Madrid, Spain Hop H Mondor A Chenevier, AP HP, Creteil, France Univ Paris Est, Fac Med, Creteil, France Univ Roma Tor Vergata, Dept Neurosci, Sect Psychiat, Rome, Italy Max Planck Inst Expt Med, Dept Neurogenet, D-37075 Gottingen, Germany Nord Biosci, Herlev, Denmark Radboud Univ Nijmegen, Med Ctr, Dept Epidemiol & Biostat, NL-6525 ED Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Urol, NL-6525 ED Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6525 ED Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Psychiat, Donders Inst Brain Cognit & Behav, NL-6525 ED Nijmegen, Netherlands Univ Med Ctr, Rudolf Magnus Inst Neurosci, Dept Neurol, Utrecht, Netherlands Kings Coll London, Inst Psychiat, Dept Child & Adolescent Psychiat, London, England Radboud Univ Nijmegen, Dept Cognit Neurosci, NL-6525 ED Nijmegen, Netherlands Goethe Univ Frankfurt, Dept Child & Adolescent Psychiat Psychosomat & Ps, D-60054 Frankfurt, Germany Univ Trier, Dept Neurobehav Genet, Trier, Germany Natl Univ Hosp Reykjavik, Dept Child & Adolescent Psychiat, Reykjavik, Iceland State Diagnost & Counseling Ctr, Kopavogur, Iceland Ukrainian Res Inst Social Forens Psychiat & Drug, Dept Child Adolescent Psychiat & Med Social Rehab, Kiev, Ukraine Univ Skopje, Dept Child & Adolescent Psychiat, Skopje, Macedonia Inst Mental Hlth, Belgrade, Serbia Univ Belgrade, Fac Med, Belgrade, Serbia Tbilisi State Med Univ TSMU, Dept Psychiat & Drug Addict, Tbilisi, Rep of Georgia Ilia State Univ, Social & Affect Neurosci Lab, Tbilisi, Rep of Georgia Ctr Addict & Mental Hlth CAMH, Mol Neuropsychiat & Dev Lab, Toronto, ON, Canada Prince Wales Hosp, Black Dog Inst, Randwick, NSW 2031, Australia Univ New S Wales, Sch Psychiat, Sydney, NSW, Australia Neurosci Res Australia, Sydney, NSW, Australia Univ New S Wales, Sch Med Sci, Sydney, NSW, Australia Queensland Inst Med Res, Brisbane, Qld 4006, Australia Catholic Univ Louvain, Univ Psychiat Ctr, Kortenberg, Belgium Maastricht Univ, European Grad Sch Neurosci EURON,Med Ctr, Sch Mental Hlth & Neurosci,Dept Psychiat & Psycho, South Limburg Mental Hlth Res & Teaching Network, Maastricht, Netherlands Semmelweis Univ, Dept Psychiat & Psychotherapy, H-1085 Budapest, Hungary Karolinska Hosp & Inst, HUBIN Project, Dept Clin Neurosci, Stockholm, Sweden Univ Med Ctr, Rudolf Magnus Inst Neurosci, Dept Psychiat, Utrecht, Netherlands Maastricht Univ, Dept Psychiat, Med Ctr, Maastricht, Netherlands Univ Western Australia, Graylands Hosp, CCRN, Perth, WA 6009, Australia UCL, Mental Hlth Sci Unit, London, England UCL, Inst Cognit Neurosci, London, England South London & Maudsley NHS Fdn Trust, NIHR Biomed Res Ctr Mental Hlth, Dept Psychosis Studies, London, England Trinity Coll Dublin, Sch Med, Neuropsychiat Genet Res Grp, Dublin, Ireland Queens Univ Belfast, Dept Psychiat, Belfast, Antrim, North Ireland Virginia Commonwealth Univ, Dept Human Genet, Richmond, VA USA Virginia Commonwealth Univ, Virginia Inst Psychiat & Behav Genet, Richmond, VA USA Virginia Commonwealth Univ, Dept Psychiat, Richmond, VA USA Cardiff Univ, Sch Med, Inst Psychol Med & Clin Neurosci, MRC Ctr Neuropsychiat Genet & Genom, Cardiff CF10 3AX, S Glam, Wales Univ Santiago de Compostela, Biomed Network Res Ctr Rare Dis CIBERER, Galician Fdn Genom Med, Genom Med Grp, Santiago De Compostela, Spain Aarhus Univ Hosp, Ctr Psychiat Res, Risskov, Denmark Aarhus Univ, Natl Ctr Register Based Res, Aarhus, Denmark German Ctr Neurodegenerat Disorders DZNE, Bonn, Germany Univ Bonn, Inst Human Genet, Bonn, Germany Inst Neurosci & Med INM 1, Julich, Germany Univ Verona, Sect Psychiat, I-37100 Verona, Italy Broad Inst MIT & Harvard, Program Med & Populat Genet & Genet Anal Platform, Cambridge, MA USA Univ Helsinki, Dept Med Genet, Helsinki, Finland Univ Cent Hosp, Helsinki, Finland Univ Halle Wittenberg, Dept Psychiat, D-06108 Halle, Germany Eli Lilly & Co Ltd, Erl Wood Manor, Windlesham, Surrey, England

مصطلحات موضوعية: Adult, Aged, 80 and over, Bipolar Disorder, Chromosome Aberrations, Chromosomes, Human, Pair 16, Europe, Female, Gene Expression Profiling, Genetic Predisposition to Disease, Genome-Wide Association Study, Genotype, Humans, International Cooperation, Male, Middle Aged, Odds Ratio, Oligonucleotide Array Sequence Analysis, Polymorphism, Single Nucleotide, Risk Factors, Schizophrenia, Young Adult

العلاقة: info:eu-repo/grantAgreement/EC/FP7/218251; http://dx.doi.org/10.1038/mp.2012.157Test; http://www.nature.com/mp/journal/v19/n1/full/mp2012157a.htmlTest; http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3872086Test/; Mol. Psychiatry 2014, 19(1):108-14; http://hdl.handle.net/2336/326288Test; Molecular psychiatry

الإتاحة: https://doi.org/10.1038/mp.2012.157Test
http://hdl.handle.net/2336/326288Test

المؤلفون: Su, Zhan, Gay, Laura, Strange, Amy, Palles, Claire, Band, Gavin, Whiteman, David, Lescai, Francesco, Langford, Cordelia, Nanji, Manoj, Brown, Matthew, other, and

المصدر: Nature Genetics

مصطلحات موضوعية: Adult, Aged, Barrett esophagus, Case-Control Studies, Chromosomes, FOXF1 gene, Gene Frequency, Genetic, Genetic Loci, Genetic Predisposition to Disease, Genome-Wide Association Study, Human, Humans, Linkage Disequilibrium, Middle Aged, Models, Pair 16, Polymorphism, Single Nucleotide, allele, article, chromosome 6p, controlled study, female, gene, gene locus, genetic association, genetic predisposition, genetic risk, genetic susceptibility

وصف الملف: application/pdf

العلاقة: https://eprints.qut.edu.au/89327/1/__qut.edu.au_Documents_StaffHome_StaffGroupB%24_bakerj2_Desktop_ukmss-49738%20%281%29.pdfTest; Su, Zhan, Gay, Laura, Strange, Amy, Palles, Claire, Band, Gavin, Whiteman, David, Lescai, Francesco, Langford, Cordelia, Nanji, Manoj, Brown, Matthew, & other, and (2012) Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus. Nature Genetics, 44(10), pp. 1131-1136.; https://eprints.qut.edu.au/89327Test/; Faculty of Health; Institute of Health and Biomedical Innovation

الإتاحة: https://doi.org/10.1038/ng.2408Test
https://eprints.qut.edu.au/89327Test/

المؤلفون: Jacquemont, Sébastien, Reymond, Alexandre, Zufferey, Flore, Harewood, Louise, Walters, Robin G, Kutalik, Zoltán, Martinet, Danielle, Shen, Yiping, Valsesia, Armand, Beckmann, Noam D, Thorleifsson, Gudmar, Männik, Katrin, Platt, Orah S, Jonveaux, Philippe, Sanlaville, Damien, Van Haelst, Mieke M, Villatoro Gomez, Sergi, Walha, Faida, Wu, Bai-Lin, Yu, Yongguo, Aboura, Azzedine, Labalme, Audrey, Addor, Marie-Claude, Alembik, Yves, Antonarakis, Stylianos E, Kaksonen, Satu, Arveiler, Benoît, Barth, Magalie, Bednarek, Nathalie, Béna, Frédérique, Bergmann, Sven, Beri, Mylène, Landais, Emilie, Bernardini, Laura, Blaumeiser, Bettina, Bonneau, Dominique, Bottani, Armand, Keren, Boris, Boute, Odile, Brunner, Han G, Cailley, Dorothée, Callier, Patrick, Chiesa, Jean, Belfiore, Marco, Chrast, Jacqueline, Coin, Lachlan, Coutton, Charles, Cuisset, Jean-Marie, Cuvellier, Jean-Christophe, Kloss-Brandstätter, Anita, David, Albert, de Freminville, Bénédicte, Delobel, Bruno, Delrue, Marie-Ange, Lapi, Elisabetta, Demeer, Bénédicte, Descamps, Dominique, Didelot, Gérard, Dieterich, Klaus, Disciglio, Vittoria, Doco-Fenzy, Martine, Knoers, Nine V A M, Drunat, Séverine, Duban-Bedu, Bénédicte, Dubourg, Christèle, Layet, Valérie, El-Sayed Moustafa, Julia S, Elliott, Paul, Faas, Brigitte H W, Faivre, Laurence, Faudet, Anne, Fellmann, Florence, Ferrarini, Alessandra, Koolen, David A, Fisher, Richard, Flori, Elisabeth, Legallic, Solenn, Forer, Lukas, Gaillard, Dominique, Gerard, Marion, Gieger, Christian, Gimelli, Stefania, Gimelli, Giorgio, Grabe, Hans J, Guichet, Agnès, Kroisel, Peter M, Guillin, Olivier, Leheup, Bruno, Hartikainen, Anna-Liisa, Heron, Délphine, Hippolyte, Loyse, Holder, Muriel, Homuth, Georg, Isidor, Bertrand, Jaillard, Sylvie, Jaros, Zdenek, Jiménez-Murcia, Susana, Kronenberg, Florian, Leube, Barbara, Helas, Géraldine Joly, Lewis, Suzanne, Lucas, Josette, Fernández-Real, José Manuel, MacDermot, Kay D, Magnusson, Pall, Marshall, Christian, Bouquillon, Sonia, Mathieu-Dramard, Michèle, McCarthy, Mark I, Meitinger, Thomas, Mencarelli, Maria Antonietta, Merla, Giuseppe, Moerman, Alexandre, Gratacòs, Mònica, Mooser, Vincent, Morice-Picard, Fanny, Mucciolo, Mafalda, Nauck, Matthias, Campion, Dominique, Ndiaye, Ndeye Coumba, Nordgren, Ann, Pasquier, Laurent, Petit, Florence, Pfundt, Rolph, Guilmatre, Audrey, Plessis, Ghislaine, Rajcan-Separovic, Evica, Ramelli, Gian Paolo, Rauch, Anita, Ravazzolo, Roberto, de Leeuw, Nicole, Reis, Andre, Renieri, Alessandra, Richart, Cristobal, Ried, Janina S, Hoyer, Juliane, Rieubland, Claudine, Roberts, Wendy, Roetzer, Katharina M, Rooryck, Caroline, Rossi, Massimiliano, Saemundsen, Evald, de Vries, Bert B A, Satre, Véronique, Schurmann, Claudia, Sigurdsson, Engilbert, Jarvelin, Marjo-Riitta, Stavropoulos, Dimitri J, Stefansson, Hreinn, Tengström, Carola, Thorsteinsdóttir, Unnur, Tinahones, Francisco J, Touraine, Renaud, Vallée, Louis, Esko, Tõnu, van Binsbergen, Ellen, Van der Aa, Nathalie, Kooy, R Frank, Vincent-Delorme, Catherine, Visvikis-Siest, Sophie, Vollenweider, Peter, Völzke, Henry, Vulto-van Silfhout, Anneke T, Waeber, Gérard, Wallgren-Pettersson, Carina, Witwicki, Robert M, Fernandez, Bridget A, Zwolinksi, Simon, Kurg, Ants, Andrieux, Joris, Estivill, Xavier, Gusella, James F, Gustafsson, Omar, Metspalu, Andres, Scherer, Stephen W, Stefansson, Kari, Blakemore, Alexandra I F, Beckmann, Jacques S, Fernández-Aranda, Fernando, Le Caignec, Cédric, Froguel, Philippe

المساهمون: Service of Medical Genetics, Centre Hospitalier Universitaire Vaudois, 1011 Lausanne, Switzerland.

مصطلحات موضوعية: Adolescent, Adult, Aged, Aging, Body Height, Body Mass Index, Case-Control Studies, Child, Preschool, Chromosomes, Human, Pair 16, Cohort Studies, Comparative Genomic Hybridization, Developmental Disabilities, Energy Metabolism, Europe, Female, Gene Dosage, Gene Duplication, Gene Expression Profiling, Genetic Predisposition to Disease, Genome-Wide Association Study, Head, Heterozygote, Humans, Infant, Newborn, Male, Mental Disorders

العلاقة: info:eu-repo/grantAgreement/EC/FP7/223423; http://dx.doi.org/10.1038/nature10406Test; http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3637175Test/; Nature 2011, 478(7367):97-102; http://hdl.handle.net/2336/225819Test; Nature

الإتاحة: https://doi.org/10.1038/nature10406Test
http://hdl.handle.net/2336/225819Test

المؤلفون: S Zhang, Masashi Fujitani, Ryosuke Fujiki, Yoshitaka Fujihara, Toshihide Yamashita

المصدر: Molecular Psychiatry

مصطلحات موضوعية: 0301 basic medicine, Cellular differentiation, Transgene, Developmental Disabilities, Neurogenesis, Protocadherin, Mice, Transgenic, Hyperkinesis, 03 medical and health sciences, Cellular and Molecular Neuroscience, Mice, Risk Factors, Gene Duplication, Gene duplication, microRNA, Animals, Humans, Genetic Predisposition to Disease, Molecular Biology, Gene, Genetics, Cell Differentiation, Cadherins, Phenotype, Protocadherins, Psychiatry and Mental health, MicroRNAs, 030104 developmental biology, Attention Deficit Disorder with Hyperactivity, Original Article, Psychology, Chromosomes, Human, Pair 16, Signal Transduction

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4efe3522b754365738186c0e4e105feaTest
http://europepmc.org/articles/PMC5322274Test